ASSOCIATION OF BILATERAL RADIOULNAR SYNOSTOSIS WITH OSTEOGENESIS IMPERFECTA TYPE 1 – CASE PRESENTATION

ASSOCIATION OF BILATERAL RADIOULNAR SYNOSTOSIS WITH OSTEOGENESIS IMPERFECTA TYPE 1 – CASE PRESENTATION

Osteogenesis imperfecta (OI) is a group of rare congenital conditions characterized mainly by bone brittleness secondary to mutations in the genes encoding collagen. The medical history together with a clinical examination in detail of the fractures is highly important in directing the diagnosis t...

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Bibliographic Details
Main Authors: Valeriu V. Lupu, Mirabela Subotnicu, Ancuța Ignat, Gabriela Păduraru, Irina Naumcieff, Bogdan Ciubară, Marin Burlea
Format: Article
Language:English
Published: Romanian Society of Oral Rehabilitation 2016-01-01
Series:Romanian Journal of Oral Rehabilitation
Subjects:
child
congenital radioulnar synostosis
osteogenesis imperfecta
Online Access:http://www.rjor.ro/association-of-bilateral-radioulnar-synostosis-with-osteogenesis-imperfecta-type-1-case-presentation/?lang=ro

Internet

http://www.rjor.ro/association-of-bilateral-radioulnar-synostosis-with-osteogenesis-imperfecta-type-1-case-presentation/?lang=ro

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